Canonical Allele Identifier: CA337554026
Gene: TBL1Y HGNC NCBI

Linked Data

dbSNP Id: rs186143316
gnomAD v3: Y-6980112-G-T
gnomAD v4: Y-6980112-G-T
MyVariant Identifiers: chrY:g.6848153G>T (hg19) chrY:g.6980112G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.6980112G>T , CM000686.2:g.6980112G>T GRCh38
NC_000024.9:g.6848153G>T , CM000686.1:g.6848153G>T GRCh37
NC_000024.8:g.6908153G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000383032.6:c.-235+1869G>T MANE Select ENSP00000372499.1:n.-235+1869G>T
ENST00000346432.3:c.-140+1869G>T ENSP00000328879.4:n.-140+1869G>T
ENST00000355162.6:c.-234-15692G>T ENSP00000347289.2:n.-234-15692G>T
ENST00000383032.5:c.-235+1869G>T ENSP00000372499.1:n.-235+1869G>T
NM_033284.1:c.-235+1869G>T NP_150600.1:n.-235+1869G>T
NM_134258.1:c.-234-15692G>T NP_599020.1:n.-234-15692G>T
NM_134259.1:c.-140+1869G>T NP_599021.1:n.-140+1869G>T
XM_017030086.1:c.-235+1869G>T XP_016885575.1:n.-235+1869G>T
XM_017030087.1:c.-235+1869G>T XP_016885576.1:n.-235+1869G>T
XM_024452497.1:c.-235+1869G>T XP_024308265.1:n.-235+1869G>T
NM_033284.2:c.-235+1869G>T MANE Select NP_150600.1:n.-235+1869G>T
NM_134258.2:c.-234-15692G>T NP_599020.1:n.-234-15692G>T
NM_134259.2:c.-140+1869G>T NP_599021.1:n.-140+1869G>T
Search 100 bp 5'
Search 100 bp 3'